Involvement of the N‐terminus of Bax in its intracellular localization and function
Open Access
- 15 January 2002
- journal article
- Published by Wiley in FEBS Letters
- Vol. 512 (1-3), 95-100
- https://doi.org/10.1016/s0014-5793(02)02227-5
Abstract
We have identified, using site‐directed mutagenesis, a proline located at position 13 of Baxα (Bax) as crucial for the maintenance of its cytosolic conformation. The substitution of this proline by a valine results in a strong binding of Bax to mitochondria and to conformational changes monitored by a decreased sensitivity of Bax to mild proteolysis and the enhancement of its oligomerization state. Deletion of the C‐terminus of Bax does not modify its intracellular localization. On the other hand, the pro‐apoptotic activity of Bax is enhanced by a deletion of the C‐terminus in the absence of the N‐terminus but is decreased in its presence. These results suggest that both extremities functionally interact to control the activity but not the subcellular localization of Bax.Keywords
This publication has 31 references indexed in Scilit:
- Conformational change of Bax: a question of life or deathCell Death & Differentiation, 2001
- BID-dependent and BID-independent pathways for BAX insertion into mitochondriaCell Death & Differentiation, 2000
- Structure of BaxCell, 2000
- Cleavage of Bax Enhances Its Cell Death FunctionExperimental Cell Research, 2000
- Role of the C‐terminal domain of Bax and Bcl‐xL in their localization and function in yeast cellsFEBS Letters, 1999
- Movement of Bax from the Cytosol to Mitochondria during ApoptosisThe Journal of cell biology, 1997
- APOPTOSIS AND DISEASE: Regulation and Clinical Relevance of Programmed Cell DeathAnnual Review of Medicine, 1997
- Programmed Cell Death in Animal DevelopmentCell, 1997
- The E1B 19K protein blocks apoptosis by interacting with and inhibiting the p53-inducible and death-promoting Bax protein.Genes & Development, 1996
- Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programed cell deathCell, 1993